70518-1556 : Divalproex Sodium 250 mg Oral Tablet, Extended Release


NDC: 70518-1556
Labeler: Remedyrepack Inc.
Product Type: Human Prescription Drug
Drug Name:  Divalproex Sodium
Dosage Form: Oral Tablet, Extended Release
Application #: ANDA203730
Rev. Date: 


Appearance:


Markings: AN;755
Shapes:  Round
Colors:  White
Size (mm): 11
Segments: * 1

* Segments = the number of equally sized pieces which the pill can be broken into. In this case, a value of 1 indicates a solid pill with no score lines.

NDC Package Codes:

  • 70518-1556-0: 30 TABLET, EXTENDED RELEASE IN 1 BLISTER PACK (70518‑1556‑0)
  • 70518-1556-1: 100 POUCH IN 1 BOX (70518‑1556‑1) > 1 TABLET, EXTENDED RELEASE IN 1 POUCH (70518‑1556‑2)
  • 70518-1556-3: 100 POUCH IN 1 BOX (70518‑1556‑3) > 1 TABLET, EXTENDED RELEASE IN 1 POUCH (70518‑1556‑4)
  • 70518-1556-5: 30 TABLET, EXTENDED RELEASE IN 1 BLISTER PACK (70518‑1556‑5)

Active Ingredients:

  • Divalproex Sodium

Dosage Strength:

  • 250 mg

Inactive Ingredients:

  • Ammonia
  • Ethyl Acrylate
  • Methacrylic Acid - Methyl Methacrylate Copolymer (1:1)
  • Hypromelloses
  • Ferrosoferric Oxide
  • Isopropyl Alcohol
  • Lactose Monohydrate
  • Polyethylene Glycol, Unspecified
  • Magnesium Stearate
  • Cellulose, Microcrystalline
  • Butyl Alcohol
  • Polyvinyl Alcohol, Unspecified
  • Propylene Glycol
  • Shellac
  • Silicon Dioxide
  • Talc
  • Titanium Dioxide /

Pharmaceutical Classes:

  • Anti-epileptic Agent [EPC]
  • Decreased Central Nervous System Disorganized Electrical Activity [PE]
  • Mood Stabilizer [EPC]

Related Products:

Based on records with the same trade name.
  • 70518-0282 Divalproex Sodium 500 mg Oral Tablet, Delayed Release by Remedyrepack Inc.
  • 70518-0312 Divalproex Sodium 250 mg Oral Tablet, Extended Release by Remedyrepack Inc.
  • 70518-0374 Divalproex Sodium 125 mg Oral Tablet, Delayed Release by Remedyrepack Inc.
  • 70518-0463 Divalproex Sodium 250 mg Oral Tablet, Delayed Release by Remedyrepack Inc.
  • 70518-0613 Divalproex Sodium 500 mg Oral Tablet, Extended Release by Remedyrepack Inc.
  • 70518-1138 Divalproex Sodium 250 mg Oral Tablet, Extended Release by Remedyrepack Inc.
  • 70518-1558 Divalproex Sodium 500 mg Oral Tablet, Delayed Release by Remedyrepack Inc.
  • 70518-1661 Divalproex Sodium 500 mg Oral Tablet, Extended Release by Remedyrepack Inc.
  • 70518-1749 Divalproex Sodium 125 mg Oral Capsule, Coated Pellets by Remedyrepack Inc.
  • 70518-1781 Divalproex Sodium 250 mg Oral Tablet, Film Coated, Extended Release by Remedyrepack Inc.
  • 70518-1897 Divalproex Sodium 500 mg Oral Tablet, Film Coated, Extended Release by Remedyrepack Inc.
  • 70518-2003 Divalproex Sodium 500 mg Oral Tablet, Film Coated, Extended Release by Remedyrepack Inc.
  • 70518-2017 Divalproex Sodium 125 mg Oral Tablet, Delayed Release by Remedyrepack Inc.
  • 70518-2033 Divalproex Sodium 500 mg Oral Tablet, Film Coated, Extended Release by Remedyrepack Inc.
  • 70518-2036 Divalproex Sodium 500 mg Oral Tablet, Extended Release by Remedyrepack Inc.
  • 70518-2357 Divalproex Sodium 500 mg Oral Tablet, Delayed Release by Remedyrepack Inc.
  • 70518-2510 Divalproex Sodium 500 mg Oral Tablet, Extended Release by Remedyrepack Inc.
  • 70518-2513 Divalproex Sodium 250 mg Oral Tablet, Delayed Release by Remedyrepack Inc.
  • 70518-2527 Divalproex Sodium 125 mg Oral Capsule, Coated Pellets by Remedyrepack Inc.
  • 70518-2626 Divalproex Sodium 500 mg Oral Tablet, Delayed Release by Remedyrepack Inc.
  • More related products ...

NDC QR Code

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Note: The RxChat NDC Database uses publicly available data from the FDA and the U.S. National Library of Medicine (NLM); The NLM is not responsible for the data presented and does not endorse or recommend this or any other product. While we make every effort to ensure that the information presented is accurate, you should assume that all results are unvalidated. To report any errors or inconsistencies please contact us.